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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 21876 - 21900 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000218765a-Tetrahydrocorticosterone,4TMS,isomer#1JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS638.4038Standard non polar3183.8916
RI000218775a-Tetrahydrocorticosterone,4TMS,isomer#2JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS638.4038Standard non polar3083.4695
RI000218785a-Tetrahydrocorticosterone,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS806.5916Standard non polar3984.0264
RI000218795a-Tetrahydrocorticosterone,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS806.5916Standard non polar3858.9104
RI000218805a-TetrahydrocorticosteroneJsmol[H][C@@]12CC[C@H](C(=O)CO)[C@@]1(C)C[C@H](O)[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@H](O)CC[C@]12CUnderivatized350.2457Standard non polar3055.3794
RI000218815a-TetrahydrocorticosteroneJsmol[H][C@@]12CC[C@H](C(=O)CO)[C@@]1(C)C[C@H](O)[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@H](O)CC[C@]12CUnderivatized350.2457Semi standard non polar3228.1575
RI000218825a-Tetrahydrocorticosterone,4TMS,isomer#1JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS638.4038Semi standard non polar3014.0225
RI000218835a-Tetrahydrocorticosterone,4TMS,isomer#2JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS638.4038Semi standard non polar3057.6948
RI000218845a-Tetrahydrocorticosterone,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS806.5916Semi standard non polar3851.8289
RI000218855a-Tetrahydrocorticosterone,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS806.5916Semi standard non polar3882.0898
RI000218865a-Tetrahydrocorticosterone,4TMS,isomer#1JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS638.4038Standard polar3346.4258
RI000218875a-Tetrahydrocorticosterone,4TMS,isomer#2JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS638.4038Standard polar3401.1042
RI000218885a-Tetrahydrocorticosterone,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS806.5916Standard polar3664.3237
RI000218895a-Tetrahydrocorticosterone,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS806.5916Standard polar3680.5918
RI000218905-Hydroxylysine,1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H](CN)CC[C@H](N)C(=O)OTMS234.14Semi standard non polar1719.6028
RI000218915-Hydroxylysine,1TMS,isomer#2JsmolC[Si](C)(C)OC(=O)[C@@H](N)CC[C@@H](O)CNTMS234.14Semi standard non polar1659.8732
RI000218925-Hydroxylysine,1TMS,isomer#3JsmolC[Si](C)(C)NC[C@H](O)CC[C@H](N)C(=O)OTMS234.14Semi standard non polar1798.7335
RI000218935-Hydroxylysine,1TMS,isomer#4JsmolC[Si](C)(C)N[C@@H](CC[C@@H](O)CN)C(=O)OTMS234.14Semi standard non polar1776.1584
RI000218945-Hydroxylysine,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@@H](N)CC[C@H](CN)O[Si](C)(C)CTMS306.1795Semi standard non polar1698.6842
RI000218955-Hydroxylysine,2TMS,isomer#2JsmolC[Si](C)(C)NC[C@@H](CC[C@H](N)C(=O)O)O[Si](C)(C)CTMS306.1795Semi standard non polar1804.8248
RI000218965-Hydroxylysine,2TMS,isomer#3JsmolC[Si](C)(C)N[C@@H](CC[C@H](CN)O[Si](C)(C)C)C(=O)OTMS306.1795Semi standard non polar1798.6688
RI000218975-Hydroxylysine,2TMS,isomer#4JsmolC[Si](C)(C)N[C@@H](CC[C@@H](O)CN)C(=O)O[Si](C)(C)CTMS306.1795Semi standard non polar1733.1526
RI000218985-Hydroxylysine,2TMS,isomer#5JsmolC[Si](C)(C)NC[C@H](O)CC[C@H](N)C(=O)O[Si](C)(C)CTMS306.1795Semi standard non polar1778.967
RI000218995-Hydroxylysine,2TMS,isomer#6JsmolC[Si](C)(C)NC[C@H](O)CC[C@H](N[Si](C)(C)C)C(=O)OTMS306.1795Semi standard non polar1879.7375
RI000219005-Hydroxylysine,2TMS,isomer#7JsmolC[Si](C)(C)N(C[C@H](O)CC[C@H](N)C(=O)O)[Si](C)(C)CTMS306.1795Semi standard non polar1963.495
Displaying retention index compounds 21876 - 21900 of 1722868 in total